Sclerosing bone dysplasias: genetic, clinical and radiology update of hereditary and non-hereditary disorders

被引:39
作者
Boulet, Cedric [1 ]
Madani, Hardi [2 ]
Lenchik, Leon [3 ]
Vanhoenacker, Filip [4 ]
Amalnath, Deepak S. [5 ]
De Mey, Johan [1 ]
De Maeseneer, Michel [1 ]
机构
[1] Univ Ziekenhuis Brussel, Dept Radiol, Brussels, Belgium
[2] Royal Free Hosp, Dept Radiol, Pond St, London NW3 2QG, England
[3] Wake Forest Univ, Dept Radiol, Winston Salem, NC 27109 USA
[4] Univ Ziekenhuis Anwerpen, Dept Radiol, Antwerp, Belgium
[5] Indira Gandhi Med Coll & Res Inst, Dept Med, Pondicherry, India
关键词
OSTEOPATHIA STRIATA; CRANIAL SCLEROSIS; RIBBING DISEASE; FEATURES; OSTEOPETROSIS; OSTEOSCLEROSIS; DIAGNOSIS; MUTATION;
D O I
10.1259/bjr.20150349
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
There is a wide variety of hereditary and non-hereditary bone dysplasias, many with unique radiographic findings. Hereditary bony dysplasias include osteopoikilosis, osteopathia striata, osteopetrosis, progressive diaphyseal dysplasia, hereditary multiple diaphyseal sclerosis and pyknodysostosis. Non-hereditary dysplasias include melorheostosis, intramedullary osteosclerosis and overlap syndromes. Although many of these dysplasias are uncommon, radiologists should be familiar with their genetic, clinical and imaging findings to allow for differentiation from acquired causes of bony sclerosis. We present an overview of hereditary and non-hereditary bony dysplasias with focus on the pathogenesis, clinical and radiographic findings of each disorder.
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相关论文
共 26 条
[1]   Camurati-Engelmann disease: imaging, clinical features and differential diagnosis [J].
Bartuseviciene, Aldona ;
Samuilis, Arturas ;
Skucas, Jovitas .
SKELETAL RADIOLOGY, 2009, 38 (11) :1037-1043
[2]   Intramedullary osteosclerosis: Imaging features in nine patients [J].
Chanchairujira, K ;
Chung, CB ;
Lai, YM ;
Haghighi, P ;
Resnick, D .
RADIOLOGY, 2001, 220 (01) :225-230
[3]   Albers-Schonberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the CICN7chloride channel gene [J].
Cleiren, E ;
Bénichou, O ;
Van Hul, E ;
Gram, J ;
Bollerslev, J ;
Singer, FR ;
Beaverson, K ;
Aledo, A ;
Whyte, MP ;
Yoneyama, T ;
deVernejoul, MC ;
Van Hul, W .
HUMAN MOLECULAR GENETICS, 2001, 10 (25) :2861-2867
[4]   Heritable sclerosing bone disorders Presentation and new molecular mechanisms [J].
de Vernejoul, Marie-Christine ;
Kornak, Uwe .
SKELETAL BIOLOGY AND MEDICINE, 2010, 1192 :269-277
[5]   AUTOSOMAL RECESSIVE OSTEOPETROSIS - BONE-MARROW IMAGING [J].
ELSTER, AD ;
THEROS, EG ;
KEY, LL ;
STANTON, C .
RADIOLOGY, 1992, 182 (02) :507-514
[6]   A Novel WTX Mutation in a Female Patient With Osteopathia Striata With Cranial Sclerosis and Hepatoblastoma [J].
Fujita, Atsushi ;
Ochi, Nobuhiko ;
Fujimaki, Hidehiko ;
Muramatsu, Hideki ;
Takahashi, Yoshiyuki ;
Natsume, Jun ;
Kojima, Seiji ;
Nakashima, Mitsuko ;
Tsurusaki, Yoshinori ;
Saitsu, Hirotomo ;
Matsumoto, Naomichi ;
Miyake, Noriko .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (04) :998-1002
[7]   SCLEROSING BONE DYSPLASIAS - A TARGET-SITE APPROACH [J].
GREENSPAN, A .
SKELETAL RADIOLOGY, 1991, 20 (08) :561-583
[8]   Sclerosing Bone Dysplasias: Review and Differentiation from Other Causes of Osteosclerosis [J].
Ihde, Lauren L. ;
Forrester, Deborah M. ;
Gottsegen, Christopher J. ;
Masih, Sulabha ;
Patel, Dakshesh B. ;
Vachon, Linda A. ;
White, Eric A. ;
Matcuk, George R., Jr. .
RADIOGRAPHICS, 2011, 31 (07) :1865-1882
[9]   Camurati-Engelmann disease:: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment [J].
Janssens, K ;
Vanhoenacker, F ;
Bonduelle, M ;
Verbruggen, L ;
Van Maldergem, L ;
Ralston, S ;
Guañabens, N ;
Migone, N ;
Wientroub, S ;
Divizia, MT ;
Bergmann, C ;
Bennett, C ;
Simsek, S ;
Melançon, S ;
Cundy, T ;
Van Hul, W .
JOURNAL OF MEDICAL GENETICS, 2006, 43 (01) :1-11
[10]  
KOLAWOLE TM, 1988, EUR J RADIOL, V8, P89